Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9930012K11Rik |
A |
T |
14: 70,393,635 (GRCm39) |
I287N |
probably benign |
Het |
Aco2 |
G |
T |
15: 81,787,820 (GRCm39) |
E223D |
probably damaging |
Het |
Acsf3 |
T |
A |
8: 123,539,770 (GRCm39) |
I466N |
probably damaging |
Het |
Albfm1 |
G |
A |
5: 90,719,625 (GRCm39) |
|
probably null |
Het |
Aox3 |
T |
A |
1: 58,191,761 (GRCm39) |
F438I |
probably benign |
Het |
Arhgap33 |
T |
C |
7: 30,225,794 (GRCm39) |
T591A |
probably benign |
Het |
Ash1l |
C |
T |
3: 88,888,694 (GRCm39) |
A191V |
probably benign |
Het |
Btg2 |
T |
C |
1: 134,006,779 (GRCm39) |
K5E |
probably benign |
Het |
C1galt1 |
T |
A |
6: 7,871,150 (GRCm39) |
Y329N |
probably damaging |
Het |
Cacna1h |
A |
G |
17: 25,608,435 (GRCm39) |
I824T |
possibly damaging |
Het |
Carmil3 |
A |
G |
14: 55,731,817 (GRCm39) |
I182V |
probably benign |
Het |
Ccdc150 |
T |
A |
1: 54,302,496 (GRCm39) |
|
probably null |
Het |
Chek1 |
T |
A |
9: 36,633,939 (GRCm39) |
R129W |
probably damaging |
Het |
Chrna6 |
A |
G |
8: 27,896,815 (GRCm39) |
M354T |
possibly damaging |
Het |
Cpq |
A |
G |
15: 33,250,185 (GRCm39) |
T181A |
probably benign |
Het |
Defb28 |
T |
A |
2: 152,361,974 (GRCm39) |
C45S |
possibly damaging |
Het |
Dnah1 |
A |
G |
14: 31,018,551 (GRCm39) |
Y1360H |
probably benign |
Het |
Dnah7c |
T |
C |
1: 46,823,608 (GRCm39) |
V3749A |
possibly damaging |
Het |
Dnah7c |
T |
A |
1: 46,819,935 (GRCm39) |
D3728E |
probably benign |
Het |
Dym |
G |
A |
18: 75,196,245 (GRCm39) |
|
probably null |
Het |
Dync2i2 |
G |
A |
2: 29,928,341 (GRCm39) |
P95L |
probably benign |
Het |
Dzip3 |
A |
G |
16: 48,747,903 (GRCm39) |
|
probably null |
Het |
Eef1akmt4 |
A |
G |
16: 20,436,666 (GRCm39) |
K163E |
probably benign |
Het |
Fbrs |
A |
G |
7: 127,081,985 (GRCm39) |
T242A |
possibly damaging |
Het |
Fgfr3 |
G |
A |
5: 33,885,146 (GRCm39) |
V87M |
possibly damaging |
Het |
Fst |
A |
T |
13: 114,595,068 (GRCm39) |
C19S |
probably benign |
Het |
Gm7276 |
G |
A |
18: 77,273,216 (GRCm39) |
R173W |
unknown |
Het |
Gm9195 |
G |
A |
14: 72,697,929 (GRCm39) |
H1284Y |
probably benign |
Het |
Herc6 |
C |
A |
6: 57,581,074 (GRCm39) |
T258K |
probably damaging |
Het |
Hip1r |
A |
G |
5: 124,137,174 (GRCm39) |
Y678C |
probably damaging |
Het |
Ifne |
A |
T |
4: 88,798,243 (GRCm39) |
N58K |
probably damaging |
Het |
Ighv1-26 |
A |
T |
12: 114,752,163 (GRCm39) |
H60Q |
possibly damaging |
Het |
Ints1 |
A |
G |
5: 139,746,520 (GRCm39) |
F1276L |
probably damaging |
Het |
Itprid2 |
A |
T |
2: 79,466,416 (GRCm39) |
D82V |
probably damaging |
Het |
Kcnc4 |
T |
A |
3: 107,366,100 (GRCm39) |
E36V |
probably benign |
Het |
Kcnq2 |
C |
T |
2: 180,750,895 (GRCm39) |
G315S |
probably damaging |
Het |
Kdm4c |
G |
A |
4: 74,255,200 (GRCm39) |
V585M |
probably damaging |
Het |
Klhl26 |
C |
T |
8: 70,905,592 (GRCm39) |
R106H |
probably damaging |
Het |
Kmo |
T |
C |
1: 175,481,221 (GRCm39) |
F313S |
probably damaging |
Het |
Lmtk3 |
T |
A |
7: 45,443,740 (GRCm39) |
S808T |
unknown |
Het |
Lrch3 |
A |
G |
16: 32,815,363 (GRCm39) |
T585A |
probably benign |
Het |
Lrch4 |
T |
A |
5: 137,637,977 (GRCm39) |
H86Q |
|
Het |
Map3k20 |
A |
G |
2: 72,195,062 (GRCm39) |
D113G |
probably damaging |
Het |
Mbd3l1 |
T |
C |
9: 18,396,417 (GRCm39) |
S181P |
probably benign |
Het |
Mccc2 |
T |
C |
13: 100,104,241 (GRCm39) |
T303A |
probably benign |
Het |
Med27 |
A |
G |
2: 29,303,490 (GRCm39) |
R147G |
possibly damaging |
Het |
Mrps5 |
T |
A |
2: 127,437,762 (GRCm39) |
S196R |
possibly damaging |
Het |
Muc21 |
GGGGTGGGCATAGATCCTGAGGCAGAGCTGGATGCAGTGGTGGTCAGGGTGGG |
GGGGTGGG |
17: 35,932,935 (GRCm39) |
|
probably benign |
Het |
Myo16 |
A |
T |
8: 10,526,185 (GRCm39) |
|
probably null |
Het |
Nudt2 |
A |
T |
4: 41,477,575 (GRCm39) |
M19L |
probably benign |
Het |
Pcdha11 |
C |
T |
18: 37,146,245 (GRCm39) |
P779S |
probably benign |
Het |
Phykpl |
A |
G |
11: 51,489,530 (GRCm39) |
T379A |
probably benign |
Het |
Plekha8 |
A |
C |
6: 54,601,206 (GRCm39) |
M270L |
probably benign |
Het |
Plekhg5 |
A |
G |
4: 152,192,885 (GRCm39) |
H593R |
probably benign |
Het |
Polr2a |
T |
C |
11: 69,637,196 (GRCm39) |
N293S |
possibly damaging |
Het |
Pramel32 |
G |
A |
4: 88,548,184 (GRCm39) |
P74S |
probably benign |
Het |
Prex2 |
T |
A |
1: 11,232,532 (GRCm39) |
N866K |
probably benign |
Het |
Psme4 |
A |
T |
11: 30,757,790 (GRCm39) |
I308L |
probably benign |
Het |
Ptprb |
T |
C |
10: 116,177,309 (GRCm39) |
V1003A |
probably benign |
Het |
Rbbp8 |
T |
A |
18: 11,865,269 (GRCm39) |
D719E |
probably damaging |
Het |
Rnaset2b |
A |
T |
17: 7,259,166 (GRCm39) |
D144V |
probably benign |
Het |
Senp6 |
T |
G |
9: 80,033,481 (GRCm39) |
D662E |
probably damaging |
Het |
Serpinb3c |
T |
C |
1: 107,200,817 (GRCm39) |
N200S |
possibly damaging |
Het |
Serpinb9g |
C |
G |
13: 33,672,543 (GRCm39) |
Y113* |
probably null |
Het |
Sgf29 |
T |
C |
7: 126,270,821 (GRCm39) |
I134T |
probably benign |
Het |
Sh3bp4 |
T |
G |
1: 89,080,824 (GRCm39) |
|
probably null |
Het |
Stab1 |
G |
A |
14: 30,862,783 (GRCm39) |
L2243F |
probably damaging |
Het |
Sympk |
T |
C |
7: 18,769,770 (GRCm39) |
V149A |
probably benign |
Het |
Syt3 |
C |
T |
7: 44,041,953 (GRCm39) |
Q271* |
probably null |
Het |
Tas2r109 |
A |
G |
6: 132,957,663 (GRCm39) |
I89T |
probably benign |
Het |
Tgif1 |
A |
G |
17: 71,151,847 (GRCm39) |
S255P |
probably damaging |
Het |
Tm9sf1 |
G |
A |
14: 55,875,432 (GRCm39) |
|
probably benign |
Het |
Tnf |
A |
G |
17: 35,419,347 (GRCm39) |
F161S |
possibly damaging |
Het |
Topaz1 |
T |
A |
9: 122,579,428 (GRCm39) |
S779R |
possibly damaging |
Het |
Topors |
A |
G |
4: 40,260,540 (GRCm39) |
S915P |
unknown |
Het |
Tpm4 |
C |
T |
8: 72,900,321 (GRCm39) |
L161F |
probably damaging |
Het |
Trim38 |
C |
T |
13: 23,975,384 (GRCm39) |
T441I |
probably damaging |
Het |
Trpv1 |
A |
G |
11: 73,141,620 (GRCm39) |
M548V |
probably benign |
Het |
Vmn2r68 |
T |
A |
7: 84,883,042 (GRCm39) |
T237S |
probably benign |
Het |
Zc3hav1 |
A |
G |
6: 38,309,209 (GRCm39) |
S538P |
probably benign |
Het |
Zfp541 |
C |
T |
7: 15,813,294 (GRCm39) |
T649I |
probably benign |
Het |
|
Other mutations in Csmd2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00519:Csmd2
|
APN |
4 |
128,377,266 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01098:Csmd2
|
APN |
4 |
127,952,845 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01114:Csmd2
|
APN |
4 |
128,262,923 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01364:Csmd2
|
APN |
4 |
128,308,081 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01530:Csmd2
|
APN |
4 |
128,308,094 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01582:Csmd2
|
APN |
4 |
128,457,098 (GRCm39) |
nonsense |
probably null |
|
IGL01670:Csmd2
|
APN |
4 |
128,407,164 (GRCm39) |
splice site |
probably benign |
|
IGL01707:Csmd2
|
APN |
4 |
128,276,798 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL01810:Csmd2
|
APN |
4 |
128,374,638 (GRCm39) |
splice site |
probably benign |
|
IGL01837:Csmd2
|
APN |
4 |
128,313,363 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01924:Csmd2
|
APN |
4 |
128,453,740 (GRCm39) |
missense |
unknown |
|
IGL02013:Csmd2
|
APN |
4 |
128,215,116 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL02020:Csmd2
|
APN |
4 |
128,453,672 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02037:Csmd2
|
APN |
4 |
128,371,263 (GRCm39) |
splice site |
probably benign |
|
IGL02303:Csmd2
|
APN |
4 |
128,262,801 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02317:Csmd2
|
APN |
4 |
128,357,520 (GRCm39) |
splice site |
probably benign |
|
IGL02322:Csmd2
|
APN |
4 |
128,357,520 (GRCm39) |
splice site |
probably benign |
|
IGL02338:Csmd2
|
APN |
4 |
128,288,859 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02412:Csmd2
|
APN |
4 |
128,407,165 (GRCm39) |
splice site |
probably benign |
|
IGL02428:Csmd2
|
APN |
4 |
128,368,609 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02491:Csmd2
|
APN |
4 |
128,428,050 (GRCm39) |
missense |
probably benign |
|
IGL02701:Csmd2
|
APN |
4 |
128,389,934 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02801:Csmd2
|
APN |
4 |
128,445,868 (GRCm39) |
splice site |
probably null |
|
IGL02818:Csmd2
|
APN |
4 |
128,103,521 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02863:Csmd2
|
APN |
4 |
128,415,677 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02876:Csmd2
|
APN |
4 |
128,215,128 (GRCm39) |
nonsense |
probably null |
|
IGL02977:Csmd2
|
APN |
4 |
128,387,069 (GRCm39) |
nonsense |
probably null |
|
IGL03006:Csmd2
|
APN |
4 |
128,374,558 (GRCm39) |
splice site |
probably benign |
|
IGL03032:Csmd2
|
APN |
4 |
128,412,834 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03148:Csmd2
|
APN |
4 |
128,278,062 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03157:Csmd2
|
APN |
4 |
128,308,092 (GRCm39) |
nonsense |
probably null |
|
IGL03245:Csmd2
|
APN |
4 |
128,402,915 (GRCm39) |
missense |
probably benign |
0.12 |
IGL03376:Csmd2
|
APN |
4 |
128,411,464 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03014:Csmd2
|
UTSW |
4 |
128,190,222 (GRCm39) |
missense |
probably benign |
0.01 |
R0109:Csmd2
|
UTSW |
4 |
128,438,536 (GRCm39) |
missense |
probably benign |
0.03 |
R0112:Csmd2
|
UTSW |
4 |
128,389,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R0157:Csmd2
|
UTSW |
4 |
128,415,704 (GRCm39) |
missense |
probably benign |
0.02 |
R0390:Csmd2
|
UTSW |
4 |
128,027,466 (GRCm39) |
intron |
probably benign |
|
R0441:Csmd2
|
UTSW |
4 |
128,414,023 (GRCm39) |
missense |
probably benign |
0.00 |
R0519:Csmd2
|
UTSW |
4 |
128,380,798 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0743:Csmd2
|
UTSW |
4 |
128,007,469 (GRCm39) |
missense |
probably benign |
0.00 |
R0746:Csmd2
|
UTSW |
4 |
128,308,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R0973:Csmd2
|
UTSW |
4 |
128,389,981 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1019:Csmd2
|
UTSW |
4 |
128,415,807 (GRCm39) |
missense |
probably benign |
0.00 |
R1476:Csmd2
|
UTSW |
4 |
128,380,794 (GRCm39) |
missense |
probably benign |
0.08 |
R1641:Csmd2
|
UTSW |
4 |
128,377,188 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1709:Csmd2
|
UTSW |
4 |
128,389,988 (GRCm39) |
missense |
probably damaging |
0.96 |
R2866:Csmd2
|
UTSW |
4 |
128,308,185 (GRCm39) |
critical splice donor site |
probably null |
|
R2870:Csmd2
|
UTSW |
4 |
128,451,511 (GRCm39) |
missense |
unknown |
|
R2870:Csmd2
|
UTSW |
4 |
128,451,511 (GRCm39) |
missense |
unknown |
|
R2871:Csmd2
|
UTSW |
4 |
128,451,511 (GRCm39) |
missense |
unknown |
|
R2871:Csmd2
|
UTSW |
4 |
128,451,511 (GRCm39) |
missense |
unknown |
|
R2872:Csmd2
|
UTSW |
4 |
128,451,511 (GRCm39) |
missense |
unknown |
|
R2872:Csmd2
|
UTSW |
4 |
128,451,511 (GRCm39) |
missense |
unknown |
|
R2873:Csmd2
|
UTSW |
4 |
128,451,511 (GRCm39) |
missense |
unknown |
|
R2893:Csmd2
|
UTSW |
4 |
128,432,786 (GRCm39) |
splice site |
probably null |
|
R3796:Csmd2
|
UTSW |
4 |
128,411,388 (GRCm39) |
missense |
probably benign |
0.20 |
R3797:Csmd2
|
UTSW |
4 |
128,411,388 (GRCm39) |
missense |
probably benign |
0.20 |
R3798:Csmd2
|
UTSW |
4 |
128,411,388 (GRCm39) |
missense |
probably benign |
0.20 |
R3914:Csmd2
|
UTSW |
4 |
128,215,117 (GRCm39) |
missense |
probably benign |
0.07 |
R4198:Csmd2
|
UTSW |
4 |
128,404,717 (GRCm39) |
missense |
probably benign |
0.07 |
R4489:Csmd2
|
UTSW |
4 |
128,275,738 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4571:Csmd2
|
UTSW |
4 |
128,373,888 (GRCm39) |
splice site |
probably null |
|
R4581:Csmd2
|
UTSW |
4 |
128,262,881 (GRCm39) |
missense |
probably benign |
0.02 |
R4599:Csmd2
|
UTSW |
4 |
127,881,921 (GRCm39) |
missense |
probably benign |
0.35 |
R4649:Csmd2
|
UTSW |
4 |
128,439,866 (GRCm39) |
missense |
probably benign |
|
R4706:Csmd2
|
UTSW |
4 |
128,438,544 (GRCm39) |
missense |
probably benign |
|
R4776:Csmd2
|
UTSW |
4 |
128,336,685 (GRCm39) |
missense |
probably benign |
0.09 |
R4838:Csmd2
|
UTSW |
4 |
128,411,542 (GRCm39) |
missense |
probably benign |
|
R4900:Csmd2
|
UTSW |
4 |
128,346,318 (GRCm39) |
missense |
probably benign |
0.03 |
R4999:Csmd2
|
UTSW |
4 |
128,415,723 (GRCm39) |
missense |
probably benign |
0.00 |
R5024:Csmd2
|
UTSW |
4 |
128,215,141 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5034:Csmd2
|
UTSW |
4 |
127,952,901 (GRCm39) |
missense |
probably damaging |
0.98 |
R5152:Csmd2
|
UTSW |
4 |
128,445,828 (GRCm39) |
missense |
probably benign |
0.27 |
R5172:Csmd2
|
UTSW |
4 |
128,371,190 (GRCm39) |
missense |
probably benign |
0.10 |
R5231:Csmd2
|
UTSW |
4 |
128,439,842 (GRCm39) |
missense |
probably benign |
0.00 |
R5279:Csmd2
|
UTSW |
4 |
128,350,707 (GRCm39) |
missense |
probably benign |
0.30 |
R5287:Csmd2
|
UTSW |
4 |
128,380,677 (GRCm39) |
missense |
probably benign |
0.01 |
R5403:Csmd2
|
UTSW |
4 |
128,380,677 (GRCm39) |
missense |
probably benign |
0.01 |
R5410:Csmd2
|
UTSW |
4 |
128,442,612 (GRCm39) |
missense |
probably benign |
|
R5551:Csmd2
|
UTSW |
4 |
128,404,741 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5566:Csmd2
|
UTSW |
4 |
128,356,682 (GRCm39) |
critical splice donor site |
probably null |
|
R5826:Csmd2
|
UTSW |
4 |
128,412,992 (GRCm39) |
splice site |
probably null |
|
R5907:Csmd2
|
UTSW |
4 |
128,091,178 (GRCm39) |
missense |
probably damaging |
0.99 |
R5913:Csmd2
|
UTSW |
4 |
128,445,781 (GRCm39) |
missense |
probably benign |
0.01 |
R5970:Csmd2
|
UTSW |
4 |
128,439,944 (GRCm39) |
missense |
probably benign |
0.00 |
R5977:Csmd2
|
UTSW |
4 |
127,952,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R6027:Csmd2
|
UTSW |
4 |
128,453,739 (GRCm39) |
missense |
unknown |
|
R6075:Csmd2
|
UTSW |
4 |
128,380,658 (GRCm39) |
missense |
probably benign |
0.15 |
R6129:Csmd2
|
UTSW |
4 |
128,387,127 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6363:Csmd2
|
UTSW |
4 |
128,294,172 (GRCm39) |
missense |
probably benign |
0.00 |
R6366:Csmd2
|
UTSW |
4 |
128,377,245 (GRCm39) |
missense |
probably benign |
0.00 |
R6404:Csmd2
|
UTSW |
4 |
128,415,743 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6437:Csmd2
|
UTSW |
4 |
127,881,893 (GRCm39) |
missense |
probably benign |
0.24 |
R6441:Csmd2
|
UTSW |
4 |
128,288,757 (GRCm39) |
missense |
probably benign |
0.03 |
R6643:Csmd2
|
UTSW |
4 |
128,266,390 (GRCm39) |
missense |
probably benign |
0.14 |
R6724:Csmd2
|
UTSW |
4 |
128,457,164 (GRCm39) |
missense |
probably damaging |
0.97 |
R6734:Csmd2
|
UTSW |
4 |
128,357,606 (GRCm39) |
missense |
probably benign |
0.00 |
R6750:Csmd2
|
UTSW |
4 |
128,091,018 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6801:Csmd2
|
UTSW |
4 |
128,277,743 (GRCm39) |
missense |
probably benign |
0.11 |
R6842:Csmd2
|
UTSW |
4 |
128,402,952 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6843:Csmd2
|
UTSW |
4 |
128,357,587 (GRCm39) |
missense |
probably benign |
0.27 |
R6868:Csmd2
|
UTSW |
4 |
128,336,633 (GRCm39) |
missense |
probably benign |
|
R6882:Csmd2
|
UTSW |
4 |
128,343,062 (GRCm39) |
missense |
probably benign |
0.01 |
R7019:Csmd2
|
UTSW |
4 |
128,262,856 (GRCm39) |
missense |
|
|
R7028:Csmd2
|
UTSW |
4 |
128,171,021 (GRCm39) |
missense |
|
|
R7096:Csmd2
|
UTSW |
4 |
128,356,519 (GRCm39) |
missense |
|
|
R7122:Csmd2
|
UTSW |
4 |
128,343,020 (GRCm39) |
missense |
|
|
R7125:Csmd2
|
UTSW |
4 |
128,389,955 (GRCm39) |
missense |
|
|
R7197:Csmd2
|
UTSW |
4 |
128,404,826 (GRCm39) |
missense |
|
|
R7234:Csmd2
|
UTSW |
4 |
128,350,572 (GRCm39) |
missense |
|
|
R7299:Csmd2
|
UTSW |
4 |
128,422,055 (GRCm39) |
missense |
|
|
R7301:Csmd2
|
UTSW |
4 |
128,422,055 (GRCm39) |
missense |
|
|
R7331:Csmd2
|
UTSW |
4 |
128,458,021 (GRCm39) |
splice site |
probably null |
|
R7332:Csmd2
|
UTSW |
4 |
128,313,360 (GRCm39) |
missense |
|
|
R7352:Csmd2
|
UTSW |
4 |
128,451,429 (GRCm39) |
missense |
|
|
R7402:Csmd2
|
UTSW |
4 |
128,215,889 (GRCm39) |
missense |
|
|
R7402:Csmd2
|
UTSW |
4 |
128,215,888 (GRCm39) |
missense |
|
|
R7474:Csmd2
|
UTSW |
4 |
128,439,920 (GRCm39) |
missense |
|
|
R7555:Csmd2
|
UTSW |
4 |
128,346,251 (GRCm39) |
missense |
|
|
R7592:Csmd2
|
UTSW |
4 |
128,357,591 (GRCm39) |
missense |
|
|
R7700:Csmd2
|
UTSW |
4 |
128,439,549 (GRCm39) |
splice site |
probably null |
|
R7714:Csmd2
|
UTSW |
4 |
128,276,743 (GRCm39) |
nonsense |
probably null |
|
R7734:Csmd2
|
UTSW |
4 |
128,445,850 (GRCm39) |
missense |
|
|
R7735:Csmd2
|
UTSW |
4 |
128,350,723 (GRCm39) |
critical splice donor site |
probably null |
|
R7757:Csmd2
|
UTSW |
4 |
128,377,249 (GRCm39) |
missense |
|
|
R7805:Csmd2
|
UTSW |
4 |
128,313,366 (GRCm39) |
missense |
|
|
R7823:Csmd2
|
UTSW |
4 |
128,103,698 (GRCm39) |
missense |
|
|
R7904:Csmd2
|
UTSW |
4 |
128,313,346 (GRCm39) |
missense |
|
|
R7946:Csmd2
|
UTSW |
4 |
128,414,058 (GRCm39) |
missense |
|
|
R7964:Csmd2
|
UTSW |
4 |
128,417,303 (GRCm39) |
missense |
|
|
R7968:Csmd2
|
UTSW |
4 |
128,091,118 (GRCm39) |
missense |
|
|
R8003:Csmd2
|
UTSW |
4 |
128,432,980 (GRCm39) |
nonsense |
probably null |
|
R8071:Csmd2
|
UTSW |
4 |
128,287,331 (GRCm39) |
missense |
|
|
R8504:Csmd2
|
UTSW |
4 |
128,440,483 (GRCm39) |
missense |
|
|
R8511:Csmd2
|
UTSW |
4 |
128,262,692 (GRCm39) |
missense |
|
|
R8517:Csmd2
|
UTSW |
4 |
128,446,479 (GRCm39) |
missense |
|
|
R8704:Csmd2
|
UTSW |
4 |
128,091,147 (GRCm39) |
missense |
|
|
R8722:Csmd2
|
UTSW |
4 |
128,445,743 (GRCm39) |
unclassified |
probably benign |
|
R8729:Csmd2
|
UTSW |
4 |
128,356,638 (GRCm39) |
missense |
|
|
R8801:Csmd2
|
UTSW |
4 |
128,457,195 (GRCm39) |
missense |
probably damaging |
0.97 |
R8803:Csmd2
|
UTSW |
4 |
128,440,477 (GRCm39) |
missense |
|
|
R8839:Csmd2
|
UTSW |
4 |
128,336,681 (GRCm39) |
missense |
|
|
R8867:Csmd2
|
UTSW |
4 |
128,451,469 (GRCm39) |
missense |
|
|
R8913:Csmd2
|
UTSW |
4 |
128,417,351 (GRCm39) |
missense |
|
|
R8928:Csmd2
|
UTSW |
4 |
128,369,582 (GRCm39) |
missense |
|
|
R8974:Csmd2
|
UTSW |
4 |
128,446,380 (GRCm39) |
missense |
|
|
R9001:Csmd2
|
UTSW |
4 |
128,308,079 (GRCm39) |
missense |
|
|
R9132:Csmd2
|
UTSW |
4 |
128,443,007 (GRCm39) |
missense |
|
|
R9245:Csmd2
|
UTSW |
4 |
128,200,168 (GRCm39) |
missense |
|
|
R9249:Csmd2
|
UTSW |
4 |
128,313,323 (GRCm39) |
nonsense |
probably null |
|
R9254:Csmd2
|
UTSW |
4 |
128,091,112 (GRCm39) |
missense |
|
|
R9265:Csmd2
|
UTSW |
4 |
128,294,163 (GRCm39) |
missense |
|
|
R9407:Csmd2
|
UTSW |
4 |
128,442,613 (GRCm39) |
missense |
|
|
R9432:Csmd2
|
UTSW |
4 |
128,171,004 (GRCm39) |
missense |
|
|
R9559:Csmd2
|
UTSW |
4 |
128,438,561 (GRCm39) |
missense |
|
|
R9673:Csmd2
|
UTSW |
4 |
128,308,062 (GRCm39) |
missense |
|
|
R9735:Csmd2
|
UTSW |
4 |
128,402,901 (GRCm39) |
missense |
|
|
R9749:Csmd2
|
UTSW |
4 |
128,389,921 (GRCm39) |
missense |
|
|
R9803:Csmd2
|
UTSW |
4 |
128,262,986 (GRCm39) |
missense |
|
|
Z1177:Csmd2
|
UTSW |
4 |
128,424,590 (GRCm39) |
missense |
|
|
|